Dynorphin in pro-opiomelanocortin neurons of the hypothalamic arcuate nucleus

被引:24
|
作者
Maolood, N. [1 ]
Meister, B. [1 ]
机构
[1] Karolinska Inst, Retzius Lab, Dept Neurosci, SE-17177 Stockholm, Sweden
关键词
body weight; food intake; arcuate nucleus; hypothalamus; melanocortin; opioid peptide;
D O I
10.1016/j.neuroscience.2008.04.011
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Considerable evidence suggests that dynorphin participates in the regulation of energy balance. In this study, we have used immunohistochemistry to investigate in detail the cellular localization of pro-dynorphin (DYN) immunoreactive cell bodies in the mediobasal hypothalamus with special reference to neurons producing orexigenic or anorexigenic transmitters. In colchicine-treated rats, DYN immunoreactivity was demonstrated in many cell bodies of the arcuate nucleus (Arc). Double-labeling revealed that DYN immunoreactivity was present in approximately 30% of pro-opiomelanocortin (POMC) neurons in the ventrolateral Arc as shown by presence of alpha-melanocyte-stimulating hormone (alpha-MSH) and cocaine- and amphetamine-regulated transcript (CART). In contrast, DYN immunoreactivity was not demonstrated in agouti-related peptide (AgRP)- or neuropeptide Y (NPY) -containing neurons in the ventromedial aspect of the Arc. Dynorphin immunoreactivity was also colocalized with the vesicular acetylcholine (ACh) transporter (VAChT; a marker for cholinergic neurons) in the cell soma of Arc POMC neurons. Brainstem POMC neurons in the commissural part of the solitary tract nucleus (NTS) were devoid of DYN immunoreactivity, whereas DYN immunoreactivity was detected in a few NPY-containing NTS neurons and cholinergic DMX neurons. Our results showing presence of DYN together with alpha-MSH in a subpopulation of hypothalamic POMC neurons further point to the neurochemical heterogeneity of hypothalamic POMC neurons. The results suggest a role for DYN in control of energy balance by mediating the effect of peripheral hormones such as leptin and insulin. (c) 2008 IBRO. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1121 / 1131
页数:11
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